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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1963705생성일: 2026년 10월 24일

Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → tert-butyl-4-(N-{4-[4-(methylamino)-3-nitrophenoxy]-2-pyridyl}carbamoyl)piperidinecarboxylate

https://huagongshe.com/ko/reaction/1963705

반응식

참여 물질

역할이름HCID투입량
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
반응물[4-(2-Amino(4-pyridyloxy))-2-nitrophenyl]methylamineHCID 69006232—
용매DimethylformamideHCID 6228—
생성물tert-butyl-4-(N-{4-[4-(methylamino)-3-nitrophenoxy]-2-pyridyl}carbamoyl)piperidinecarboxylateHCID 69038249—

반응 단계

To a mixture of 1-(tert-butoxy)carbonylpiperidine-4-carboxylic acid (1 eq) in N,N-dimethyl formamide and N,N-disopropylethylamine (4 eq) was added BOP (2 eq) and the mixture was stirred at ambient temperature until homogeneous. To it was added [4-(2-amino(4-pyridyloxy))-2-nitrophenyl]methylamine (1 eq) and the resulting mixture was stirred at 60° C. for 16 h. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was dried over sodium sulfate and the resulting tert-butyl-4-(N-{4-[4-(methylamino)-3-nitrophenoxy]-2-pyridyl}carbamoyl)piperidinecarboxylate was purified by silica gel chromatography. MS: MH+=472.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08415382B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-9d0fa942aa18481bb5415e11a6c1960f
출처 메모uspto-grants-2013_04